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T19720Colcemid；秋水仙碱C 12669|||C-12669|||NSC-3096|||Kolchicin|||C12669|||Demecolcine；C 12669|||C-12669|||NSC
Colcemid (NSC-3096) is an inhibitor of microtubule polymerization. It used to study embryonic cloning.
价 格：￥电议型 号：T19720产 地：中国大陆
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T1972GSK-5959；化合物GSK 5959GSK-5959
GSK-5959 is an effective, specific and cell permeable BRPF1 bromodomain inhibitor (IC50: ~80 nM). The selectivity of GSK-5959 for BRPF1 is >100-fold over a panel of 35 other bromodomains, including BRPF2/3 and BET family bromodomains.
价 格：￥电议型 号：T1972产 地：中国大陆
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T19719TBMP；化合物TBMPbutylated hydroxyanisole；butylated hydroxyanisole
TBMP (butylated hydroxyanisole) is the viral envelope protein hemagglutinin (HA)-mediated entry novel inhibitor.
价 格：￥电议型 号：T19719产 地：中国大陆
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T19717Cyclo-L-Trp-L-Trp；环(L-色氨酰-L-色氨酰)Cyclo-L-Trp-L-Trp
Cyclo-L-Trp-L-Trp is a broad-spectrum antifungal. It also induces a high degree of acetylation of histones.
价 格：￥电议型 号：T19717产 地：中国大陆
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T197161,3,5-Trihydroxyxanthone；化合物 T197161,3,5-Trihydroxyxanthone
1,3,5-Trihydroxyxanthone is a highly cytotoxic natural compound. It against a range of bacteria and yeasts.Anti-androgenic.
价 格：￥电议型 号：T19716产 地：中国大陆
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T19714Fenpyroximate；唑螨酯Fenpyroximate
Fenpyroximate is an acaricide and insecticide. It blocks the mitochondrial electron transport in complex I.
价 格：￥电议型 号：T19714产 地：中国大陆
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T19713HHQ；2-庚基-4-喹啉酮2-heptylquinolin-4(1H)-one；2-庚基-4-喹啉酮|||2-heptylquinolin-4(1H)-one
HHQ (2-heptylquinolin-4(1H)-one) is a PqsR antagonist.
价 格：￥电议型 号：T19713产 地：中国大陆
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T19712Levoglucosenone；左旋葡萄糖酮Levoglucosenone
Levoglucosenone has cytotoxic. It against human hepatocarcinoma cell lines.
价 格：￥电议型 号：T19712产 地：中国大陆
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T19711Desmosterol；24-脱氢胆固醇Desmesterol|||24-Dehydrocholesterol；Desmesterol|||24-Dehydrocholesterol
Desmosterol (24-Dehydrocholesterol) is a cholesterol biosynthesis intermediate that inhibits macrophage inflammatory vesicle activation and prevents vascular inflammation and atherosclerosis.
价 格：￥电议型 号：T19711产 地：中国大陆
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T19710Ciglitazone；环格列酮Ciglitazona|||U 63287|||ADD3878|||ADD-3878|||U-63287|||ADD 3878；Ciglitazona|||U 6328
Ciglitazone (ADD 3878) is a potent and selective PPARγ agonist (EC50: 3 μM) and oral hypoglycemic agent. Ciglitazone inhibits proliferation and differentiation of th17 cells, decreases insulin levels, vascular endothelial growth factor production and blood pressure, and induces cell cycle arrest in gastric cancer cells. Selegiline induces apoptosis in opossum kidney epithelial cells and activates nuclear translocation of p38 MAPK and apoptosis-inducing factor (AIF). Ciglitazone exhibits hypoglyc
价 格：￥电议型 号：T19710产 地：中国大陆
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T1971WAY-262611；化合物WAY-262611WAY-262611
WAY262611 is a Wnt/β-catenin agonist and an inhibitor of Dkk1. It increases bone formation rate with EC50 of 0.63 μM in TCF-luciferase assay.
价 格：￥电议型 号：T1971产 地：中国大陆
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T19709Nitrocefin；头孢硝噻吩Nitrocefin
Nitrocefin is an antibiotic. It being sensitive to hydrolysis by all lactamases produced by gram-positive and gram-negative bacteria.
价 格：￥电议型 号：T19709产 地：中国大陆
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T19708(S)-Warfarin化合物 T19708(S)Warfarin|||(S) Warfarin
(S)-Warfarin is a more effective enantiomer of Warfarin. It is used as a vitamin K antagonist, with anticoagulant.
价 格：￥电议型 号：T19708产 地：中国大陆
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T19707Denopamine；化合物 T19707Denopamine
Denopamine is an agonist of 1-Adrenoceptor.
价 格：￥电议型 号：T19707产 地：中国大陆
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T19706Ro 20-1724；化合物Ro20-1724Ro-20-1724|||4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone|||Ro20-1724；Ro-20
Ro 20-1724 (4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone) is a widely used inhibitor of cyclic nucleotide phosphodiesterase with IC50 of 2.0 μM and Ki of 3.1 μM.
价 格：￥电议型 号：T19706产 地：中国大陆
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T19703LG100268化合物 T19703LG 100268|||LG-100268
LG100268 is an effective and selective rexinoid and retinoid-X receptor agonist. LG100268 binds to the α, β, and γ RXR receptors (IC50 = 3-4 nM).
价 格：￥电议型 号：T19703产 地：中国大陆
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T19702L-838417；化合物 T19702L 838417；L 838417
L838417 is a modulator of the GABAA receptor.
价 格：￥电议型 号：T19702产 地：中国大陆
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T19701L-694,247；化合物 T19701L-694,247
L-694,247 is a selective and extremely potent agonist of the 5-HT1D receptor.
价 格：￥电议型 号：T19701产 地：中国大陆
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T19700IBC 293；1-异丙基-1H-1,2,3-苯并噻唑-5-羧酸IBC293|||IBC-293；IBC293|||1-异丙基-1H-1,2,3-苯并噻唑-5-羧酸|||IBC-293
IBC 293 is selective for GPR109B over niacin receptor GPR109A. IBC 293 is a highly selective agonist for GPR109B, a human orphan G-protein-coupled receptor expressed in adipocytes.
价 格：￥电议型 号：T19700产 地：中国大陆
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T1970Gedatolisib；化合物GedatolisibPF-05212384|||PKI-587；PF-05212384|||PKI-587
Gedatolisib (PF-05212384) is a highly effective dual inhibitor targeting the PI3Kα/γ (IC50: 0.4/5.4 nM)and mTOR (IC50: 1.6 nM) in the PI3K/mTOR signaling pathway.
价 格：￥电议型 号：T1970产 地：中国大陆
